NDC Package 73126-032-01 Truth Antibacterial Foaming Hand Wash - Unscented

Benzalkonium Chloride Liquid Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
73126-032-01
Package Description:
60 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Truth Antibacterial Foaming Hand Wash - Unscented
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Apply small amount of product to wet hands. Work into lather and rub briskly for 15-30 seconds. Rinse thoroughly. Dry hands.
11-Digit NDC Billing Format:
73126003201
NDC to RxNorm Crosswalk:
  • RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
  • RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
  • RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Lab-clean, Inc
    Dosage Form:
    Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    part333E
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    03-04-2021
    End Marketing Date:
    04-20-2024
    Exclude Flag:
    N

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    73126-032-0288 mL in 1 BOTTLE
    73126-032-03237 mL in 1 BOTTLE
    73126-032-04355 mL in 1 BOTTLE
    73126-032-05474 mL in 1 BOTTLE
    73126-032-06591 mL in 1 PACKAGE
    73126-032-07710 mL in 1 PACKAGE
    73126-032-08947 mL in 1 PACKAGE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 73126-032-01?

    The NDC Packaged Code 73126-032-01 is assigned to a package of 60 ml in 1 bottle of Truth Antibacterial Foaming Hand Wash - Unscented, a human over the counter drug labeled by Lab-clean, Inc. The product's dosage form is liquid and is administered via topical form.

    Is NDC 73126-032 included in the NDC Directory?

    Yes, Truth Antibacterial Foaming Hand Wash - Unscented with product code 73126-032 is active and included in the NDC Directory. The product was first marketed by Lab-clean, Inc on March 04, 2021.

    What is the 11-digit format for NDC 73126-032-01?

    The 11-digit format is 73126003201. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-273126-032-015-4-273126-0032-01